Craniofacial abnormalities and developmental delay in two families with overlapping 22q12.1 microdeletions involving the MN1 gene

Publisher： John Wiley & Sons Inc

E-ISSN： 1552-4833|167|5|1047-1053

ISSN： 1552-4825

Source： American Journal Of Medical Genetics Part A, Vol.167, Iss.5, 2015-05, pp. : 1047-1053

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Abstract

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